Canonical Allele Identifier: CA2677457447
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130670del , CM000668.2:g.18130670del GRCh38
NC_000006.11:g.18130901del , CM000668.1:g.18130901del GRCh37
NC_000006.10:g.18238880del NCBI36
NG_012137.2:g.29474del
NG_012137.3:g.29474del

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.736del MANE Select ENSP00000312304.4:p.Ter246LysextTer2
ENST00000309983.4:c.736del ENSP00000312304.4:p.Ter246LysextTer2
NM_000367.3:c.736del NP_000358.1:p.Ter246LysextTer2
XM_011514839.1:c.691del XP_011513141.1:p.Ter231LysextTer2
XM_011514840.1:c.667del XP_011513142.1:p.Ter223LysextTer2
NM_000367.4:c.736del NP_000358.1:p.Ter246LysextTer2
NM_001346817.1:c.736del NP_001333746.1:p.Ter246LysextTer2
NM_001346818.1:c.691del NP_001333747.1:p.Ter231LysextTer2
NM_000367.5:c.736del MANE Select NP_000358.1:p.Ter246LysextTer2